SCHEMBL915167

SCHEMBL915167

Cc1ccc(S(=O)(=O)O)cc1.N=C(N)N(O)/N=C/c1cccc([N+](=O)[O-])c1

nearest known ligand 0.54

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 8/20 0.54
LMNA P02545 3/20 0.54
NFE2L2 Q16236 1/20 0.47
PTGS2 P35354 1/20 0.47
RECQL P46063 2/20 0.45
L3MBTL1 Q9Y468 2/20 0.45
MAPK1 P28482 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
AGTR1 P30556 1/20 0.43
CA1 P00915 2/20 0.43
CA2 P00918 2/20 0.43
MEN1 O00255 3/20 0.43
KMT2A Q03164 3/20 0.43
CYP1A2 P05177 2/20 0.43
CYP3A4 P08684 1/20 0.43
HIF1A Q16665 1/20 0.43
HPGD P15428 1/20 0.42
MAPT P10636 3/20 0.41
MCOLN3 Q8TDD5 1/20 0.41

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL915168 1.00 ALDH1A1 (0.54) ALDH1A1LMNANFE2L2PTGS2RECQL
SCHEMBL7066006 0.87 GRIN2D (0.43) ALDH1A1LMNAPTGS2MAPK1SMN1; SMN2
SCHEMBL7066007 0.87 GRIN2D (0.43) ALDH1A1LMNAPTGS2MAPK1SMN1; SMN2
SCHEMBL7062405 0.85 CYP2D6 (0.40) ALDH1A1LMNAL3MBTL1MAPK1SMN1; SMN2
SCHEMBL7062403 0.85 CYP2D6 (0.40) ALDH1A1LMNAL3MBTL1MAPK1SMN1; SMN2
SCHEMBL915928 0.83 PTGS2 (0.47) ALDH1A1LMNAPTGS2MAPK1SMN1; SMN2
SCHEMBL915930 0.83 PTGS2 (0.47) ALDH1A1LMNAPTGS2MAPK1SMN1; SMN2
SCHEMBL7065970 0.83 CYP2D6 (0.41) ALDH1A1LMNAL3MBTL1MAPK1SMN1; SMN2
SCHEMBL7065967 0.83 CYP2D6 (0.41) ALDH1A1LMNAL3MBTL1MAPK1SMN1; SMN2
SCHEMBL7066723 0.82 ALDH1A1 (0.55) ALDH1A1LMNAMAPK1SMN1; SMN2TDP1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110015437-A1 USE OF BENZYLIDENEAMINOGUANIDINES AND HYDROXYGUANIDINES AS MELANOCORTIN RECEPTOR LIGANDS ACURE PHARMA AB (SE) 2011-01-20 US disclosed
EP-1313461-A2 THE USE OF BENZYLIDENEAMINOGUANIDINES AND HYDROXYGUANIDINES AS MELANOCORTIN RECEPTOR LIGANDS Melacure Therapeutics AB (SE) 2003-05-28 EP disclosed
WO-2002011715-A2 THE USE OF BENZYLIDENEAMINOGUANIDINES AND HYDROXYGUANIDINES AS MELANOCORTIN RECEPTOR LIGANDS MELACURE THERAPEUTICS AB (SE) 2002-02-14 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110015437-A1 USE OF BENZYLIDENEAMINOGUANIDINES AND HYDROXYGUANIDINES AS MELANOCORTIN RECEPTOR LIGANDS MC1R, MC5R, MCHR1 ALDH1A1 1879/4885LMNA 4609/4885NFE2L2 852/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.